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HomeHSNChapter 30HSN 3001 90 10

Of human origin

Dried human glands, organs and organo-therapeutic substances

WCCB CLEARANCE

HSN 3001 90 10 (Of human origin) is subject to Wildlife Crime Control Bureau (WCCB) clearance under the Wild Life (Protection) Act, 1962 and CITES provisions, which apply to human and animal biological material under this tariff line. Import of human biological material for biomedical purposes is referred to the Indian Council of Medical Research (ICMR) as the nodal implementing agency under Policy Condition 1 of Chapter 30, while drug-category consignments require a valid import licence and registration certificate uploaded in e-Sanchit.

What this is
HSN code
3001 90 10
Chapter
30 · Pharmaceutical products
Primary regulator
WCCB · Wild Life (Protection) Act, 1962 and CITES
Customs documentation
  • Registration certificate from CDSCO
  • Import licence for drugs from CDSCO
  • Certificate of Analysis from exporter
Applicable Partner Government Agencies
WCCBWCCB·Wildlife Crime Control Bureau

Procedural directions for customs clearance are issued by: Directorate General of Foreign Trade.

Compliance steps
  1. 1
    Verify WCCB and CITES compliance before shipment: the consignment must satisfy the Wild Life (Protection) Act, 1962 as amended and any applicable CITES permit requirements. For human biological material imported for biomedical research or diagnostic purposes, obtain ICMR referral clearance under Policy Condition 1 of Chapter 30 prior to filing the bill of entry.
    ITC (HS) Import Policy Condition 1 of Chapter 30 · Wild Life (Protection) Act, 1962 · CITES
  2. 2
    Ensure the following documents are uploaded in e-Sanchit before the bill of entry is processed: Certificate of Analysis — Drug (document code 0010dc), Batch Release Certificate (document code 0030dc), Label of Consignment (document code 0110dc), Registration Certificate — Drugs (document code 101dc1), and Import Licence for Drugs (document code 9111dc). Absence of any mandatory upload will prevent customs out-of-charge.
    CCR mandatory document list · e-Sanchit document codes 0010dc, 0030dc, 0110dc, 101dc1, 9111dc
A word of counsel

The most common error on this tariff line is treating the drug-licence upload as sufficient and overlooking the ICMR referral requirement for human biological material imported for biomedical purposes. These are parallel and independent obligations: a current drug import licence and a valid registration certificate satisfy the CDSCO overlay, but human biological material for biomedical use additionally requires ICMR nodal-agency clearance under Policy Condition 1 of Chapter 30 — failure to obtain it exposes the consignment to detention and referral delay at the port of entry.

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Frequently asked
Does HSN 3001 90 10 require BIS certification?
No, dried human glands and organo-therapeutic substances of human origin are not within the BIS Quality Control Order regime. Import is governed by Wildlife Crime Control Bureau clearance under the Wild Life (Protection) Act, 1962 and CITES, with a drug-licence overlay and ICMR referral for biomedical material under ITC (HS) Policy Condition 1 of Chapter 30.
Which e-Sanchit document codes are mandatory at the bill of entry for this tariff line?
Five documents must be uploaded: Certificate of Analysis — Drug (0010dc), Batch Release Certificate (0030dc), Label of Consignment (0110dc), Registration Certificate — Drugs (101dc1), and Import Licence for Drugs (9111dc). Out-of-charge will not be granted until all five are present in e-Sanchit.
When does the ICMR referral requirement apply?
ICMR referral applies specifically to human biological material imported for biomedical purposes; ICMR is the nodal implementing agency for the Ministry of Health and Family Welfare under Policy Condition 1 of Chapter 30. Import of blood and other biological material for diagnostic or therapeutic purposes in individual cases is free of this referral requirement.
Last verified against gazette notifications: 2026-05-16. Source: WCCB / DGFT / Indian Customs CUSDATA.
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